http://identifiers.org/hco/3/GRCh38#31532782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115139371-C-A

31532782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: non coding transcript exon variant
orthologous variants: 115139371-C-G

31532782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: non coding transcript exon variant
orthologous variants: 115139371-C-T

31532798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: non coding transcript exon variant
orthologous variants: 115139355-T-A

31532798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: non coding transcript exon variant
orthologous variants: 115139355-T-C

http://identifiers.org/hco/3/GRCh38#31532857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115139293-C-A

31532857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: non coding transcript exon variant
orthologous variants: 115139293-C-T

http://identifiers.org/hco/3/GRCh38#31532934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115139191-C-A

31532934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115139191-C-G

31532934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115139191-C-T

http://identifiers.org/hco/3/GRCh38#31533098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#115139023-C-A

31533098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 115139023-C-G

31533098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 115139023-C-T

31533152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115138981-A-G

31533152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 115138981-A-T

http://identifiers.org/hco/3/GRCh38#31533224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115138906-A-C

31533224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115138906-A-G

31533388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115138779-T-C

31533422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115138748-G-A

31533422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115138748-G-T

31533745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115138567-T-C

31533770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115138542-T-A

31533770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115138542-T-G

31533806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115138507-C-T

31533817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115138496-G-T

31534014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115138341-G-A

31534016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115138339-G-A

31534041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115138310-C-T

31534137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115138212-A-G

31534137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115138212-A-T

31534177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115138170-A-G

31534177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115138170-A-T

31534392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115137995-T-A

31534404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115137983-C-T

31534600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115137760-G-A

31534600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115137760-G-C

31534601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115137759-G-A

31534887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115137485-A-G

31535975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115136817-G-C

31536040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115136752-C-G

31536338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115136530-C-T

http://identifiers.org/hco/3/GRCh38#31536365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115136503-A-C

31536440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115136434-C-T

31536765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115136136-A-G

31538220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115134548-T-C

31538238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115134522-A-G

31538572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115134226-A-G

31538641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115134184-A-G

31538896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115133973-C-T

31538979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115133904-A-G

31539134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115133770-T-A

31539228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115133659-A-G

http://identifiers.org/hco/3/GRCh38#31539313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115133591-A-C

31539470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115133461-G-A

31539507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115133430-C-T

http://identifiers.org/hco/3/GRCh38#31539620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115133160-C-A

31539718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115133060-T-G

31540257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115132576-G-A

31540551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115132357-A-G

31540716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115132214-A-T

31541089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115131950-A-G

31542525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115128986-G-T

31542661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115128859-T-C

31543227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115128424-C-T

http://identifiers.org/hco/3/GRCh38#31543612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115128041-C-A

31543612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115128041-C-G

http://identifiers.org/hco/3/GRCh38#31543631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115128024-A-C

31543675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115127988-G-A

31543774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115127894-A-G

31544203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115127523-A-G

31545653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115126339-G-A

31545814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115126245-G-T

31546127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115126131-G-A

31546564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115125752-A-G

31546602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115125714-C-G

31547112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115124962-A-T

31547163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115124908-T-A

http://identifiers.org/hco/3/GRCh38#31547206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115124865-C-A

31547764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115124464-A-G

31547790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115124435-T-A

http://identifiers.org/hco/3/GRCh38#31547932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115124341-C-A

http://identifiers.org/hco/3/GRCh38#31550329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115123668-A-C

31550396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115123608-A-G

31550401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115123604-A-G

31551179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115122816-C-G

31551196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115122797-G-T

31551518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115122426-C-G

31551639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115122310-C-T

31551753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115122183-C-G

31552215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115121573-C-T

31552612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115121302-C-G

31553749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115120525-C-T

31554129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115119979-C-T

31554200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115119915-G-A

31554242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115119886-T-C

31567345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115116071-C-G

31567346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115116070-T-G

31567402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115116010-A-G

31567427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115115987-T-A

31567472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115115944-G-A

31571751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115114876-C-T

31574926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115109846-T-A

31574926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115109846-T-C

31575049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115109731-A-G

31576358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115109621-G-A

31576527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115109455-A-G

31576527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115109455-A-T

31576656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115109340-T-C

31577224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115108863-C-G

31578049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115108051-G-A

31578456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115107458-T-A

31578605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115107319-C-T

31578715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115107221-G-A

31578715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115107221-G-C

31578759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115107178-G-A

31578894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115107046-C-T

31579170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115106803-C-G

31579227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115106761-T-C

31579326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115106682-A-T

31579699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115106183-G-A

31579699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115106183-G-T

31579938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115105928-A-G

31580254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115105625-A-G

31580637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115105357-A-G

31580923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115105112-T-C

31580928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115105107-G-A

31581077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115104962-T-C

31581180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115104889-A-G

31596783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115096458-G-A

31599965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115095587-A-G

31599989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115095563-T-G

31599996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115095556-A-G

31600087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115095477-A-G

31600301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115095322-A-G

31600324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115095299-A-G

31600495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115095138-A-G

31600497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115095136-A-G

31600497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115095136-A-T

31608101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115093796-A-G

31608106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115093791-A-G

31609808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115092005-T-C

31609833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115091958-G-A

31609904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115091891-T-C

31610144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115091689-A-G

31610224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115091608-G-A

31610316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115091493-C-G

31610325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115091479-T-G

31610403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115091405-T-A

31610806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115090929-C-T

31611035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115090729-A-G

31611129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115090650-T-C

31611337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115090502-T-A

http://identifiers.org/hco/3/GRCh38#31611859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115090317-A-C

31612023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115090163-A-G

31613581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115089018-A-G

31613599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115089000-A-G

31613624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088976-C-G

31613677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088953-T-C

31613677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088953-T-G

31614401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115088214-T-C

31614988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087733-A-G

http://identifiers.org/hco/3/GRCh38#31615023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115087705-A-C

31615023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115087705-A-G

31616665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086913-T-C

31616706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086868-G-A

31616805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086771-A-G

31616805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086771-A-T

http://identifiers.org/hco/3/GRCh38#31616891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115086689-A-C

31616906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086671-A-T

31616910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086667-G-T

31617036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115086541-G-A

http://identifiers.org/hco/3/GRCh38#31617090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115086487-C-A

31617090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086487-C-T

http://identifiers.org/hco/3/GRCh38#31617103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115086474-A-C

31617103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086474-A-G

http://identifiers.org/hco/3/GRCh38#31617115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115086401-C-A

31617115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086401-C-T

http://identifiers.org/hco/3/GRCh38#31617152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115086358-C-A

31617152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086358-C-G

31617152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086358-C-T

http://identifiers.org/hco/3/GRCh38#31617211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115086285-A-C

31617211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086285-A-G

31617211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086285-A-T

31617277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086221-T-A

31617291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086208-A-T

31617376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115086149-C-G

31617856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085901-A-T

31617910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085275-A-G

31617910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085275-A-T

31617957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115085230-A-G

31617981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115085206-G-A

http://identifiers.org/hco/3/GRCh38#31617996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115085191-C-A

31617996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 115085191-C-T

31618017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085169-T-C

31618032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085158-T-C

31618063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085131-G-C

31618068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085126-T-A

http://identifiers.org/hco/3/GRCh38#31618084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115085110-C-A

31618084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085110-C-G

31618096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085101-G-C

31618104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115085093-G-T

31618558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115084700-T-C

31619105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115084337-G-A

31619342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115084304-G-T

http://identifiers.org/hco/3/GRCh38#31619616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115084072-C-A

31619880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115083812-T-G

31619905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115083791-T-C

31619947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115083774-C-G

31619983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115083741-T-C

31621538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115083578-A-G

31621639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115083514-T-C

31621675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115083491-C-T

31621851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115083325-T-C

31621960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115083236-G-A

31621960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115083236-G-T

31621993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115083207-G-A

31621997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115083203-T-G

31622060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115083144-T-C

31622065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115083139-C-T

31622421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115082775-T-C

31622430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115082766-T-G

http://identifiers.org/hco/3/GRCh38#31622440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115082756-C-A

31622902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115082414-A-G

31622928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115082388-G-T

31623207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115082171-G-T

31623360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115082037-A-G

http://identifiers.org/hco/3/GRCh38#31623527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115081878-C-A

31623618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115081801-T-C

31623657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115081768-T-A

31623785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: missense variant
orthologous variants: 115081641-G-T

31623935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115081510-A-G

http://identifiers.org/hco/3/GRCh38#31624703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115081118-A-C

31624703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115081118-A-T

31624799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115081035-A-G

31624855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115080981-A-T

31624868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115080968-C-G

31624874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115080962-T-C

31624878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115080959-A-G

31625077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: missense variant
orthologous variants: 115080752-A-G

31625090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115080733-G-T

31625094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115080729-T-G

31625114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115080703-A-G

31625160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115080660-T-A

31625267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115080604-A-T

31625454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: 115080451-C-G

http://identifiers.org/hco/3/GRCh38#31625639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115080282-C-A

31626331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115079457-T-C

31626345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115079443-C-T

31626596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115079195-A-G

31626596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115079195-A-T

31626955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115078859-T-C

31629180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115077777-A-T

31629252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115077729-T-C

http://identifiers.org/hco/3/GRCh38#31629441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115077540-C-A

31632818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115075439-T-C

31632818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115075439-T-G

31632833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115075423-T-C

31632888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115075369-A-G

31632888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115075369-A-T

31633115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115075143-A-G

31633115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115075143-A-T

31633162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115075096-A-T

31633280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115075001-T-A

31633280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115075001-T-C

31633309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115074978-T-A

31633309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115074978-T-C

31633560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115074696-T-C

http://identifiers.org/hco/3/GRCh38#31633587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115074663-C-A

31633594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115074656-A-T

31633681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115074564-A-G

31633690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115074555-T-A

31635526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115073473-A-G

31635553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115073444-A-G

31635632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115073363-G-C

31636005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115073090-T-C

31636067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115073028-G-A

http://identifiers.org/hco/3/GRCh38#31636116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115072984-C-A

31636116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115072984-C-T

http://identifiers.org/hco/3/GRCh38#31636468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115072631-C-A

31636468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3 prime UTR variant
orthologous variants: 115072631-C-G

31636468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3 prime UTR variant
orthologous variants: 115072631-C-T

31636727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3 prime UTR variant
orthologous variants: 115072379-G-T

http://identifiers.org/hco/3/GRCh38#31636883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115072225-A-C

31636883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3 prime UTR variant
orthologous variants: 115072225-A-G

31637223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3 prime UTR variant
orthologous variants: 115071889-G-A

31637223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3 prime UTR variant
orthologous variants: 115071889-G-T

31637358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30611
most severe consequence: 3 prime UTR variant
orthologous variants: 115071777-A-T