http://identifiers.org/hco/13/GRCh38#60396388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#87653338-C-A

60396388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, undefined
orthologous variants: 87653338-C-T

http://identifiers.org/hco/13/GRCh38#60396472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87653422-C-A

60396505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87653453-G-A

60396505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87653453-G-C

60396505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87653453-G-T

60396560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87653502-G-A

60396613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87653555-A-G

60396736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87653650-G-A

http://identifiers.org/hco/13/GRCh38#60396765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#87653675-C-A

60396790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87653700-G-T

http://identifiers.org/hco/13/GRCh38#60396796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#87653706-A-C

60396796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87653706-A-G

60396796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87653706-A-T

60396862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87653761-A-G

http://identifiers.org/hco/13/GRCh38#60396886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#87653785-C-A

60396886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 87653785-C-T

60396954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 87653842-G-A

60396954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 87653842-G-T

60396972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87653860-A-G

60396972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87653860-A-T

http://identifiers.org/hco/13/GRCh38#60397051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87653898-C-A

60397051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87653898-C-G

60397140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87653992-G-A

60397140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87653992-G-C

60397218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 87654070-G-A

60397218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 87654070-G-T

60397304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87654181-T-A

60397304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87654181-T-C

60397304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87654181-T-G

60397356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87654234-G-A

60397356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87654234-G-T

60397494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87654372-G-A

60397494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87654372-G-C

60397494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87654372-G-T

60397510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87654388-T-C

http://identifiers.org/hco/13/GRCh38#60397521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#87654399-C-A

60397521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 87654399-C-G

60397521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 87654399-C-T

60397640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 87654508-T-G

60397778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87654644-T-G

60398052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87654866-G-T

60398546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87655376-G-C

60399203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 87656114-C-T

60400026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87656843-T-A

60400137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87656946-T-G

60401509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87658112-T-G

60401791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87658500-G-T

60401830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87658533-A-G

http://identifiers.org/hco/13/GRCh38#60402260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87658821-A-C

60402260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87658821-A-G

60402760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87659635-C-T

http://identifiers.org/hco/13/GRCh38#60402837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87659726-C-A

60402837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87659726-C-T

60402839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87659728-C-T

60402939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87659786-A-G

60403033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87659880-T-C

60403384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87660197-G-A

60403707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87660469-G-C

60406329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87662285-T-C

60406345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87662293-G-A

60406345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87662293-G-T

60406646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87662757-G-T

60410646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87664119-A-G

60410678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87664149-A-G

60410731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87664199-A-G

60410757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87664223-G-A

60411027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87664499-G-T

http://identifiers.org/hco/13/GRCh38#60411055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87664527-A-C

60411202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87664851-C-G

60411992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87665533-T-C

60413540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87669684-A-G

60415783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87674755-G-A

60415783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87674755-G-C

60415803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87674775-C-T

http://identifiers.org/hco/13/GRCh38#60415804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87674776-A-C

60415918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87674884-A-G

60416121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87675039-G-A

60416128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87675046-C-T

60416179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87675092-G-A

60416188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87675101-C-G

60429040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87682554-C-T

60429875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87683585-C-T

http://identifiers.org/hco/13/GRCh38#60429914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87684451-A-C

60429918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87684455-T-C

60429919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87684456-G-A

60429931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87684471-A-G

60429971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87684509-A-G

60429987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87684525-A-G

60430107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87684634-G-A

60430107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87684634-G-T

60430192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87684697-G-T

60430287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87684762-C-T

60430304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87684779-C-G

60430376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87684849-A-G

60430399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87684869-A-G

60430558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87685020-C-T

60430848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87686930-T-G

60430850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87686932-A-G

60430911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87686994-A-G

60431366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87689782-A-G

60431369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87689785-G-A

60431449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87689863-A-G

http://identifiers.org/hco/13/GRCh38#60431669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87690037-A-C

60431816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87690301-G-C

60431879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87690364-T-C

60432885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87692278-A-T

http://identifiers.org/hco/13/GRCh38#60432961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87692406-C-A

60433176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87692653-A-G

60433516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87692989-C-T

60433647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87693107-A-G

60433994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87693412-A-G

60433994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87693412-A-T

60434011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87693428-A-G

60434026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87693440-C-T

http://identifiers.org/hco/13/GRCh38#60439397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87694227-A-C

60439397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87694227-A-G

60439410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87694240-C-T

60439448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87694276-A-G

60439538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87694355-T-C

60439822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87694607-T-C

60439866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87694653-A-G

60439890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87694676-T-C

60439914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87694818-G-A

60439914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87694818-G-C

60439914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87694818-G-T

60439962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87694862-A-T

60439975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87694875-T-A

60440123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87694987-G-A

60442101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87695255-A-T

http://identifiers.org/hco/13/GRCh38#60442293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87695438-C-A

60444320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87695856-A-G

60444328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87695864-G-A

60444403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87695936-G-A

http://identifiers.org/hco/13/GRCh38#60444547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87696056-A-C

60444547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87696056-A-G

60444925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87696404-T-C

60444925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87696404-T-G

60445154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87696600-A-G

60445234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87696668-T-A

http://identifiers.org/hco/13/GRCh38#60445310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87696873-C-A

60445680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87697203-A-T

60445809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87697329-A-T

http://identifiers.org/hco/13/GRCh38#60446143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87697693-A-C

60446615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87697766-G-A

60446974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87698066-C-G

60447159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87698419-A-G

60447605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699025-G-C

60447699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699103-T-G

60447740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699143-G-A

60447758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699162-A-G

http://identifiers.org/hco/13/GRCh38#60447827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87699227-A-C

60447976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699345-A-G

60447994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699363-T-G

60448040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699408-G-A

http://identifiers.org/hco/13/GRCh38#60448205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87699542-A-C

60448416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87699706-A-G

60449004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87701778-T-C

60449132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87701905-T-G

60449253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87702034-A-G

60450795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87704479-A-G

60450939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87704786-G-T

http://identifiers.org/hco/13/GRCh38#60450985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87704911-C-A

60451133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87705064-T-G

60459137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87708632-T-C

60459232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87708722-A-G

60459290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87708792-T-C

60460000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87709212-C-T

60460279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87709427-G-T

60460300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87709447-G-T

http://identifiers.org/hco/13/GRCh38#60460412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87709544-A-C

60460412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87709544-A-G

60460430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87709562-A-G

60460451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87709583-T-A

60460508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87709640-A-G

60460668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87709792-T-A

60460668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87709792-T-C

60461119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87709919-G-C

60465354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87710322-G-A

60465354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87710322-G-C

60467220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87712117-C-T

60467301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 87712198-C-T

60467436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87712306-A-G

60467480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87712353-A-G

60467486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87712358-A-G

60482347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87713306-G-C

60482540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87713488-G-T

60482691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87713656-G-A

60482783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87713753-G-A

60482783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87713753-G-C

60483064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87713993-C-T

60483624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87714687-T-A

60483624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87714687-T-C

60483624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87714687-T-G

60483720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87714767-T-C

60483743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87714791-A-G

60483843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 87714894-A-G

http://identifiers.org/hco/13/GRCh38#60483912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87714961-C-A

60483912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87714961-C-T

60483947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87715000-A-G

60484311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87716329-C-T

60484343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87716359-T-A

60484519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87716504-A-G

60484531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87716517-G-A

60484565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87716590-A-G

60484840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87717141-T-C

60484974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87717304-T-C

60485025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87717349-T-G

60485026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87717350-A-G

60485177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87717498-G-A

60485177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87717498-G-T

http://identifiers.org/hco/13/GRCh38#60485510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87717829-C-A

60485510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87717829-C-T

60485581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87717910-A-G

60485813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87718184-T-C

60485948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 87718319-A-G

60485948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 87718319-A-T

60485990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87718351-T-C

60486002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87718363-A-G

60486079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87718429-T-C

60486374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87718697-C-T

60486426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87718749-T-C

60486469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87718805-C-T

60489243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87718889-T-G

60489396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87719032-A-G

60489547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87719163-C-T

60489593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87719217-G-A

60489639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87719242-C-T

60489691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87719288-G-T

60489698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87719295-G-A

60489824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87719408-A-G

60489855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87719434-T-G

60489878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87719448-G-A

60489986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87719526-T-C

60490006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87719541-G-T

60490021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87719555-C-T

60490164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87719673-C-G

60490578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87720111-T-C

60490635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87720167-A-G

60490685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87720220-G-A

60490774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87720291-C-T

60490782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87720299-T-C

60491093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87720530-A-G

60491143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87720560-T-A

60491143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87720560-T-G

http://identifiers.org/hco/13/GRCh38#60491456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87720991-C-A

60491456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87720991-C-G

60491470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87721005-A-G

60492370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87721628-G-A

60492375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87721633-A-G

60492432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87721683-A-G

60492437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87721688-G-T

60492483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87721752-G-T

60492826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87722032-G-T

http://identifiers.org/hco/13/GRCh38#60492849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87722055-C-A

http://identifiers.org/hco/13/GRCh38#60492897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87722102-C-A

60492897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87722102-C-T

http://identifiers.org/hco/13/GRCh38#60494029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87722561-A-C

60494029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87722561-A-G

60494291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87722850-G-A

http://identifiers.org/hco/13/GRCh38#60494350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87722913-A-C

60494350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87722913-A-G

60494531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 87723091-T-A

60494554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87723114-T-C

60494610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87723177-T-C

60494624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87723197-G-A

60494624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87723197-G-T

60509502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87723405-A-G

60509597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87723468-T-C

http://identifiers.org/hco/13/GRCh38#60509598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87723469-C-A

60509598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87723469-C-T

60509641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87723517-A-T

60509816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87723681-A-G

60509819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87723684-G-A

60510057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87723881-G-A

60510533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87724434-A-G

60510667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 87724635-T-A

60510667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87724635-T-C

60510694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87724662-A-G

60510766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87724734-T-C

60510896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87724819-G-C

60511344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87725281-A-G

60515432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87726814-A-G

60515481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87726863-C-T

60515636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87727008-T-C

60515948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87727229-C-T

60516060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87727338-T-C

60516156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87727644-C-G

60518643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87728702-C-G

60518909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87728956-A-G

60518921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87728968-T-C

60519065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87729109-T-C

60519630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87730329-G-A

60519904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87730558-C-T

60519930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87730590-A-G

60520130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87730748-G-A

60520489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87731163-G-T

60520493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87731167-C-T

60520505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87731179-A-T

60520734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87731539-C-T

60520778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87731584-G-A

60520879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87731681-T-G

60520913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87731688-T-C

60521127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87731887-G-A

60521197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87731958-G-A

http://identifiers.org/hco/13/GRCh38#60521229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87731980-A-C

60521229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87731980-A-G

60521408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87732143-T-C

60521408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87732143-T-G

60522205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87733821-A-G

60522337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87733921-G-A

60522628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87734589-T-G

60522691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87734654-G-C

60522868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87734796-T-A

60522868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87734796-T-G

60522960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87734886-C-G

60522997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87734922-G-A

60526605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87742331-C-T

http://identifiers.org/hco/13/GRCh38#60527160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87742540-A-C

60527160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87742540-A-G

60527346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87742672-G-A

60527346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87742672-G-C

60527400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 87742709-A-G

60527400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 87742709-A-T

60528193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87743033-A-G

60528283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87743115-T-A

60528325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87743155-G-A

60528348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87743176-G-C

60528348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87743176-G-T

60528352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87743180-A-G

60528352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87743180-A-T

60528374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87743202-A-G

60528413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87743241-A-T

60528448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 87743276-A-G

60528555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 87743383-G-A

60528584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87743412-A-G

60528611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87743439-A-G

60528638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 87743466-T-G

60528678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 87743506-T-C

http://identifiers.org/hco/13/GRCh38#60528737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87743565-A-C

60528737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87743565-A-G

60528829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 87743657-A-T

60528885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: missense variant
orthologous variants: 87743713-A-G

60529243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87744061-C-T

60529244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87744062-A-G

60529270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87744087-A-G

60529275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87744092-G-A

60529275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87744092-G-T

60529301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87744106-A-G

60529445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87744223-T-G

http://identifiers.org/hco/13/GRCh38#60529450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87744228-C-A

60529587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87744357-A-T

60529738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87744480-C-T

60531788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87747115-T-C

60532308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87747651-A-G

60532367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87747707-C-T

60532583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87747899-T-C

60532749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87748044-C-T

60533122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87748842-A-G

60533205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87748903-G-T

60535134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87749107-C-G

60535134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87749107-C-T

60535200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87749173-G-A

60535634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87749580-T-G

60535758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87749710-A-G

60535848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87749799-G-T

60536054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87749908-A-G

60536082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87749941-G-A

60536429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87750267-T-C

60536593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87750426-C-T

60536929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87750903-T-C

60536942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87750915-T-C

60536982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87750956-A-G

60537233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87751131-G-A

60537233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87751131-G-T

60537326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87751236-A-G

60537680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87751578-G-T

http://identifiers.org/hco/13/GRCh38#60537952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87751854-A-C

http://identifiers.org/hco/13/GRCh38#60538203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87752095-C-A

60538350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87752281-C-T

60539032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87753152-A-G

60539039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87753158-T-A

60539039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87753158-T-C

60539262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87753403-C-G

http://identifiers.org/hco/13/GRCh38#60539784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87754903-C-A

60539807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87754926-G-T

http://identifiers.org/hco/13/GRCh38#60539817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87754936-A-C

http://identifiers.org/hco/13/GRCh38#60539872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87754978-A-C

60539872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87754978-A-G

60539903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87755011-G-C

http://identifiers.org/hco/13/GRCh38#60540354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87755550-A-C

60540403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87755596-C-T

60540419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87755613-T-C

60540913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87756081-T-C

60540935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87756097-C-G

60540935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87756097-C-T

60542251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87756575-T-C

60542487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87756797-T-G

60542525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87756834-G-C

60542558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87756868-A-G

60542646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87756952-A-G

60542782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87757071-C-T

60542857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87757134-T-A

60543096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87757352-G-T

60543144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87757415-G-A

60543439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87757649-A-G

60543512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87757730-A-G

http://identifiers.org/hco/13/GRCh38#60543824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87757919-A-C

60543907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87757971-T-C

60544850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87758870-C-G

60544909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87758928-C-G

60545526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87759450-G-A

60547058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87760520-C-T

http://identifiers.org/hco/13/GRCh38#60547149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87760614-C-A

http://identifiers.org/hco/13/GRCh38#60547192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87760657-C-A

60547208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87760672-A-G

60547290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, missense_variant
orthologous variants: 87760757-G-A

60547317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87760789-C-G

http://identifiers.org/hco/13/GRCh38#60547555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87761029-C-A

http://identifiers.org/hco/13/GRCh38#60547612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87761083-C-A

http://identifiers.org/hco/13/GRCh38#60547854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87761286-C-A

60548123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87761519-C-T

http://identifiers.org/hco/13/GRCh38#60548728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87762059-A-C

60548832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87762167-C-G

60548832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87762167-C-T

60549151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87762438-C-T

60549697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87763159-G-A

60549697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87763159-G-C

60549789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87763439-A-G

60549828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87763476-T-A

60550007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87763672-G-A

http://identifiers.org/hco/13/GRCh38#60550052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87763711-A-C

60550246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87763992-T-C

60550311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87764056-G-T

60550370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87764119-G-C

60550517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87764270-G-A

60550790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87764561-T-A

60550872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87764676-C-T

60551132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87765047-G-A

60551573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87765411-C-G

60553972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87765554-C-T

60554040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87765629-C-T

60554168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87765755-G-A

60555522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87766635-G-C

60555530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87766643-G-C

60555609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87766708-C-T

60555801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87766934-G-T

60556180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87767004-A-T

60556208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87767037-T-C

http://identifiers.org/hco/13/GRCh38#60556344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87767180-C-A

http://identifiers.org/hco/13/GRCh38#60556508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87767331-A-C

60557666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87768067-C-G

60558267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: -C-T

60558270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: -A-G

60558432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: -A-G

http://identifiers.org/hco/13/GRCh38#60559494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87768964-C-A

60559494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87768964-C-T

60559546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87769014-T-C

60559716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87769370-G-A

60559838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87769485-C-T

60559840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87769487-G-A

60559840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87769487-G-T

60560156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87769846-G-T

60560487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87770446-T-C

http://identifiers.org/hco/13/GRCh38#60560552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87770513-A-C

60560552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87770513-A-G

60560561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87770522-A-G

60561450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87771627-G-T

60561492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87771667-A-G

60561964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87772096-A-T

60562378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87772191-C-G

60562391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87772204-G-A

60562453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87772264-A-G

60562510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87772328-A-G

60562556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87772372-A-G

60562664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87772474-G-C

60562709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87772520-T-C

60563737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87773871-C-G

60563970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87774088-G-T

60563972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87774090-A-G

60564032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87774144-T-C

60565491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87775005-T-A

60565713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87775212-T-C

60565836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87775344-A-T

60565876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87775389-A-G

60565887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87775400-A-T

60565904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87775421-T-C

60566105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87775596-T-C

60566126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87775618-C-G

60566286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87775745-T-C

60566668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87776136-G-A

http://identifiers.org/hco/13/GRCh38#60566696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87776179-A-C

60566696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87776179-A-G

http://identifiers.org/hco/13/GRCh38#60567375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87776713-C-A

60567375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87776713-C-G

60567511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87776819-C-G

60568333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87778750-G-T

60570870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87779240-T-C

http://identifiers.org/hco/13/GRCh38#60570890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87779260-A-C

60570890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87779260-A-G

60570976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87779346-A-G

60571071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87779435-A-G

60571333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87779726-T-C

60571375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87779757-G-T

60571406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87779789-C-T

60571681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87780005-T-G

60571715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87780034-C-G

60571745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87780073-A-G

60571792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87780125-C-T

60571964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87780303-G-C

60571980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87780417-A-G

60571983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87780420-A-G

60572263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87780802-A-G

60572276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87780813-A-G

60572369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87780890-T-G

60572412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87780928-T-C

60572649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, undefined
orthologous variants: 87781093-T-C

60572659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87781099-G-T

60572856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, undefined
orthologous variants: 87781297-G-C

60572927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, undefined
orthologous variants: 87781363-T-A

60572927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron_variant, undefined
orthologous variants: 87781363-T-G

http://identifiers.org/hco/13/GRCh38#60573106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87781751-C-A

60573376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87782291-G-A

60573423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87782342-A-G

60573423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: intron variant
orthologous variants: 87782342-A-T

http://identifiers.org/hco/13/GRCh38#60573675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87782748-C-A

http://identifiers.org/hco/13/GRCh38#60573703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#87782775-C-A

60573703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3 prime UTR variant
orthologous variants: 87782775-C-G

60573704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3 prime UTR variant
orthologous variants: 87782776-T-G

60573758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20612
most severe consequence: 3 prime UTR variant
orthologous variants: 87782828-A-G