38210520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158035788-A-G

38210523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158035791-T-C

38210568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158035829-C-T

38210671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158035929-G-T

http://identifiers.org/hco/20/GRCh38#38210700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158035958-C-A

38210700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158035958-C-G

38210700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158035958-C-T

http://identifiers.org/hco/20/GRCh38#38210821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158036088-C-A

http://identifiers.org/hco/20/GRCh38#38210854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158036122-C-A

38210854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036122-C-T

http://identifiers.org/hco/20/GRCh38#38210885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158036153-C-A

38210885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036153-C-T

38210935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036244-G-A

38210935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036244-G-T

http://identifiers.org/hco/20/GRCh38#38210970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158036408-C-A

38210970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036408-C-T

38211104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036670-G-T

38211119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036689-G-A

38211119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036689-G-T

38211231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036782-G-T

38211240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036791-T-C

38211255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036802-G-A

38211255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036802-G-T

38211258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036805-C-T

38211266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036813-C-T

38211297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036843-A-G

38211305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036852-T-C

38211340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036886-G-T

http://identifiers.org/hco/20/GRCh38#38211390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158036934-C-A

38211392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158036936-T-C

38211478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037021-G-A

38212478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037410-T-C

http://identifiers.org/hco/20/GRCh38#38212487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158037418-A-C

38212487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037418-A-G

38212534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037459-T-C

38212534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037459-T-G

http://identifiers.org/hco/20/GRCh38#38212576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158037493-C-A

38212594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037511-G-A

http://identifiers.org/hco/20/GRCh38#38212634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158037528-A-C

38212638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037532-T-C

38212692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037556-G-T

http://identifiers.org/hco/20/GRCh38#38212712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158037570-C-A

38212712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037570-C-T

http://identifiers.org/hco/20/GRCh38#38212713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158037571-C-A

38212713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037571-C-T

38212743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037599-T-A

38212743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037599-T-C

38212743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037599-T-G

http://identifiers.org/hco/20/GRCh38#38212748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158037604-C-A

38212748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037604-C-G

38212748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037604-C-T

38212776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037631-G-T

http://identifiers.org/hco/20/GRCh38#38212781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158037657-A-C

38212794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037670-C-T

38212853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037738-C-T

38212882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037766-G-A

38212882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158037766-G-T

38213078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158037917-C-G

38213078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158037917-C-T

http://identifiers.org/hco/20/GRCh38#38213121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158037960-C-A

38213121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158037960-C-T

38213133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158037972-C-T

38213197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158038036-G-A

38213197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158038036-G-T

38213527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158038351-T-C

38213569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158038393-G-A

38213569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158038393-G-C

38213654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158038478-G-A

38213654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158038478-G-C

38213654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158038478-G-T

http://identifiers.org/hco/20/GRCh38#38213660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158038490-C-A

38213660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158038490-C-T

38213683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158038513-A-G

38213683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158038513-A-T

38213684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158038514-G-A

38213684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158038514-G-T

http://identifiers.org/hco/20/GRCh38#38213697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158038527-C-A

38213697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158038527-C-G

38213713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158038543-G-A

38213713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158038543-G-T

38213796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158038652-G-A

38213796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158038652-G-T

38213841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158038674-T-C

http://identifiers.org/hco/20/GRCh38#38213864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158038692-C-A

38213864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158038692-C-T

38213865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158038693-C-T

38213887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158038715-T-C

http://identifiers.org/hco/20/GRCh38#38214450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158039480-C-A

38214450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158039480-C-G

38214450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158039480-C-T

38214723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158039719-C-G

38214760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158039759-C-T

http://identifiers.org/hco/20/GRCh38#38214767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158039766-A-C

38214773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158039772-T-C

38215321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158040254-C-G

38215438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158040333-C-T

38215493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158040388-G-A

38215493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158040388-G-C

http://identifiers.org/hco/20/GRCh38#38215635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158040471-C-A

38215635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158040471-C-T

38215696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158040530-G-C

38215737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158040571-T-C

http://identifiers.org/hco/20/GRCh38#38215977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158040972-C-A

38216109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158041063-G-A

38216120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158041072-C-T

38216261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158041199-C-T

38216715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158041672-A-T

http://identifiers.org/hco/20/GRCh38#38216721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158041678-A-C

38216721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158041678-A-G

38216746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158041705-G-A

38216746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158041705-G-T

http://identifiers.org/hco/20/GRCh38#38216751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158041710-A-C

http://identifiers.org/hco/20/GRCh38#38216761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158041728-A-C

38216772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158041738-T-A

38216772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158041738-T-G

38216777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158041743-T-G

http://identifiers.org/hco/20/GRCh38#38216852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158041859-A-C

38216852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 158041859-A-T

http://identifiers.org/hco/20/GRCh38#38216916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158041919-A-C

38216959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_lost
orthologous variants: 158041934-T-G

38217380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158042201-G-A

38217398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158042210-G-A

38217404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158042216-C-T

http://identifiers.org/hco/20/GRCh38#38217500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158042303-C-A

38217500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158042303-C-T

38217518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158042316-G-A

38217518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158042316-G-T

38217563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158042348-G-A

38217563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158042348-G-T

38217581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158042356-T-A

38217581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158042356-T-C

http://identifiers.org/hco/20/GRCh38#38217683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158042422-C-A

38217715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042457-G-A

38217747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042486-G-A

38217747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042486-G-T

38217790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042510-G-C

38217790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042510-G-T

38217808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042528-T-C

38217826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042542-T-C

38217861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042564-T-C

38217861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042564-T-G

38217867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042569-T-A

38217867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042569-T-G

38217876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042578-G-A

38217876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042578-G-C

38217876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042578-G-T

http://identifiers.org/hco/20/GRCh38#38217905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#158042589-C-A

38217905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042589-C-T

38217907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042591-A-G

http://identifiers.org/hco/20/GRCh38#38217911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#158042595-C-A

http://identifiers.org/hco/20/GRCh38#38217937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#158042616-C-A

38217937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042616-C-T

http://identifiers.org/hco/20/GRCh38#38217940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#158042619-C-A

38217940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042619-C-T

38217946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042625-T-C

http://identifiers.org/hco/20/GRCh38#38217973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#158042636-C-A

38217984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042647-G-C

38218049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042708-G-T

http://identifiers.org/hco/20/GRCh38#38218095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#158042751-C-A

38218095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042751-C-T

http://identifiers.org/hco/20/GRCh38#38218109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#158042767-C-A

38218109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042767-C-T

38218119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042777-T-A

38218129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042785-T-C

http://identifiers.org/hco/20/GRCh38#38218130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#158042786-C-A

http://identifiers.org/hco/20/GRCh38#38218138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#158042794-C-A

38218138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042794-C-G

http://identifiers.org/hco/20/GRCh38#38218187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#158042839-C-A

38218187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042839-C-T

38218197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 158042850-C-T

38218276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 158042913-C-T

38218349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158042986-C-G

38218380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158043016-G-A

38218403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158043039-G-A

38218403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158043039-G-T

38219134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158044584-C-T

38219332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158044756-C-G

38219383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158044818-G-A

38219383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158044818-G-T

38219450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158044876-A-G

38219514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158044924-T-A

38219654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158045017-G-A

38219666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158045029-A-T

http://identifiers.org/hco/20/GRCh38#38219756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158045119-A-C

38219775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 158045138-G-A

38219776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 158045139-G-A

38219776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 158045139-G-C

38219780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158045143-G-A

38219780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158045143-G-C

38219860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 158045208-T-A

http://identifiers.org/hco/20/GRCh38#38219886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158045236-C-A

38219892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 158045242-G-A

38219892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158045242-G-T

http://identifiers.org/hco/20/GRCh38#38219991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158045325-C-A

38222362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158046506-G-A

38222362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158046506-G-T

38222614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158046745-G-A

38222614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158046745-G-T

http://identifiers.org/hco/20/GRCh38#38222618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158046749-C-A

http://identifiers.org/hco/20/GRCh38#38222625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158046756-C-A

38222625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158046756-C-T

http://identifiers.org/hco/20/GRCh38#38222626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158046757-C-A

38222626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158046757-C-T

38222631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158046762-C-G

38222631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158046762-C-T

http://identifiers.org/hco/20/GRCh38#38222662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158046786-C-A

38222662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158046786-C-T

http://identifiers.org/hco/20/GRCh38#38222664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158046788-C-A

38222664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158046788-C-G

38222679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158046801-G-A

38222679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158046801-G-T

http://identifiers.org/hco/20/GRCh38#38222823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158046933-C-A

38222823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158046933-C-T

38222846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158046956-G-A

38222846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158046956-G-C

38222846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158046956-G-T

http://identifiers.org/hco/20/GRCh38#38222854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#158046964-C-A

http://identifiers.org/hco/20/GRCh38#38222861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#158046971-C-A

38222861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158046971-C-T

38222926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158047061-G-T

38222927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158047062-T-C

38222961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158047082-C-T

http://identifiers.org/hco/20/GRCh38#38222972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#158047083-C-A

38222972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158047083-C-T

http://identifiers.org/hco/20/GRCh38#38222977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#158047088-C-A

38222977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158047088-C-G

38222977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158047088-C-T

38223062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158047155-C-T

38223102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158047173-G-C

38223102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158047173-G-T

http://identifiers.org/hco/20/GRCh38#38223145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158047216-A-C

http://identifiers.org/hco/20/GRCh38#38223152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158047218-C-A

38223152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047218-C-T

38223161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047230-T-C

38223173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047242-A-G

http://identifiers.org/hco/20/GRCh38#38223193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158047262-C-A

38223193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047262-C-T

http://identifiers.org/hco/20/GRCh38#38223219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158047281-C-A

http://identifiers.org/hco/20/GRCh38#38223234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158047296-C-A

38223262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047349-G-A

38223332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047418-A-G

38223391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047480-G-A

38223391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047480-G-T

38223422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047510-G-T

38223452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047532-C-T

http://identifiers.org/hco/20/GRCh38#38223453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158047533-C-A

38223453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047533-C-T

38223457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047537-G-T

http://identifiers.org/hco/20/GRCh38#38223522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158047603-C-A

38223625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158047708-A-G

38223651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047734-A-G

38223659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047742-G-A

38223659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047742-G-T

38223702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047783-T-C

http://identifiers.org/hco/20/GRCh38#38223711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158047792-C-A

38223711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047792-C-T

http://identifiers.org/hco/20/GRCh38#38223761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158047824-C-A

38223787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047847-G-T

38223794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158047854-G-A

38224043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158048098-A-G

38224283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158048321-G-A

http://identifiers.org/hco/20/GRCh38#38225293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158049933-C-A

38225293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158049933-C-T

38225297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158049937-C-T

38225298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158049938-G-A

38225298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158049938-G-C

38225436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158050114-G-T

http://identifiers.org/hco/20/GRCh38#38225459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158050128-C-A

38225459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158050128-C-T

38225520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158050188-T-C

38225528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158050196-G-T

38225560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158050228-G-A

38225560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158050228-G-T

38225572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158050240-G-C

38225572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158050240-G-T

http://identifiers.org/hco/20/GRCh38#38225613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158050288-A-C

38225613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158050288-A-G

38225648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158050316-G-A

38225648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158050316-G-T

38225671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 158050339-G-A

38225671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158050339-G-T

38225742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158050410-C-T

38225767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 158050435-G-A

http://identifiers.org/hco/20/GRCh38#38225881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158050543-A-C

38225881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158050543-A-G

38225886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158050549-T-C

38225908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158050560-A-G

38225924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158050574-A-G

38225980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158050626-G-C

38226023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158050668-T-A

http://identifiers.org/hco/20/GRCh38#38226202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158050812-C-A

38226202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158050812-C-G

38226712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158051691-T-C

http://identifiers.org/hco/20/GRCh38#38226950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158051899-C-A

38226950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158051899-C-T

38227023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158051946-A-T

38227048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158051971-G-T

38227065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158051980-G-T

38227120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158052029-C-T

38227125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158052034-C-T

http://identifiers.org/hco/20/GRCh38#38227127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158052036-C-A

38227174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 158052076-G-A

38227182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158052084-A-T

38227201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158052103-C-T

38227210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158052112-G-T

38227230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158052132-G-A

38227231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158052133-G-C

38227265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158052168-T-C

38227265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158052168-T-G

http://identifiers.org/hco/20/GRCh38#38227274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158052177-C-A

38227298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158052184-A-G

http://identifiers.org/hco/20/GRCh38#38227315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158052201-C-A

http://identifiers.org/hco/20/GRCh38#38227316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158052202-A-C

38227358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158052232-G-A

38227358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158052232-G-T

38227390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158052259-T-G

38227439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158052300-C-T

38227522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158052364-T-C

38227552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158052388-C-T

38227830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158052640-G-A

38227830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158052640-G-T

38228022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158053432-G-A

38228022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158053432-G-C

38228022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158053432-G-T

38228037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158053448-G-A

http://identifiers.org/hco/20/GRCh38#38228096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158053489-C-A

38228096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158053489-C-T

38228250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158053643-G-A

38228250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158053643-G-T

http://identifiers.org/hco/20/GRCh38#38228299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158053678-C-A

38228299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158053678-C-T

http://identifiers.org/hco/20/GRCh38#38228319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158053692-C-A

38228319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158053692-C-T

http://identifiers.org/hco/20/GRCh38#38228320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158053693-C-A

38228556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158053791-G-C

38228731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158053939-T-A

38228758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158053961-G-C

38228792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158054040-G-C

38228847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158054114-A-G

38228870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158054181-C-G

38229030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158054322-T-G

38229117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158054420-C-T

http://identifiers.org/hco/20/GRCh38#38229139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158054442-A-C

http://identifiers.org/hco/20/GRCh38#38231063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158055165-C-A

38231063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055165-C-T

38231064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055166-A-G

38231096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055197-A-G

38231099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055200-G-A

38231099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055200-G-T

38231104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055205-G-T

38231111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055212-A-G

38231133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055232-C-T

http://identifiers.org/hco/20/GRCh38#38231152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158055235-C-A

38231156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055239-A-G

http://identifiers.org/hco/20/GRCh38#38231225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158055306-C-A

38231225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158055306-C-G

38231279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158055360-T-C

38231315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158055396-G-T

38231357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055436-G-A

38231357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055436-G-C

http://identifiers.org/hco/20/GRCh38#38231373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158055451-C-A

38231373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055451-C-G

38231397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055478-G-A

38231397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055478-G-C

38231397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055478-G-T

http://identifiers.org/hco/20/GRCh38#38231415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158055496-C-A

38231415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055496-C-G

38231415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055496-C-T

38231473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055550-A-G

38231473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055550-A-T

38231848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055923-T-A

38231935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055969-G-A

38231936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055970-G-C

38231959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055993-G-A

38231962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158055996-C-T

38238309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158056748-G-A

http://identifiers.org/hco/20/GRCh38#38238392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158056815-A-C

38238448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158056870-C-T

38238718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057092-A-G

38238903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057179-G-T

38239201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057492-G-A

38239286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057549-C-T

38239305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057568-A-G

38239329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057596-G-A

38239350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057617-G-A

38239369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057636-C-G

38239433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057664-G-A

38239433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057664-G-T

38239440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057671-C-T

38239446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057681-T-C

http://identifiers.org/hco/20/GRCh38#38239449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158057684-C-A

38239449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057684-C-G

38239449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057684-C-T

38239451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057686-T-A

38239451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057686-T-C

http://identifiers.org/hco/20/GRCh38#38239452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158057687-C-A

38239547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 158057767-G-A

38239570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158057790-G-C

38239585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158057805-G-A

38239585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158057805-G-T

38239679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 158057896-G-A

38239679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158057896-G-C

38239679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158057896-G-T

38239789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057993-C-T

38239790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057994-G-A

38239790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158057994-G-T

http://identifiers.org/hco/20/GRCh38#38239807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158058008-C-A

38239807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158058008-C-T

38239820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158058023-G-T

38239835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158058034-T-A

38240365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158058186-G-A

38240440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158058245-C-G

38240558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158058332-C-T

38240607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 158058378-G-T

38240734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158058505-G-A

38240734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158058505-G-T

http://identifiers.org/hco/20/GRCh38#38240785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158058556-C-A

38240798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158058569-C-G

38240897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 158058665-G-A

38240970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 158058738-G-A

38241092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158058860-G-T

38241173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158058941-T-A

38241255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 158059023-C-T

38241411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 158059179-T-C

38241459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 158059227-G-A

38241459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158059227-G-T

38241677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158059445-C-T

38241716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158059484-G-C

38241716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 158059484-G-T

38242016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158059790-T-C

38242090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158059876-T-C

38242186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158059970-G-A

38242340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158060109-T-G

38242422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158060197-T-A

38242422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158060197-T-C

38245133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158061664-C-T

38245137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158061668-G-A

http://identifiers.org/hco/20/GRCh38#38245151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158061682-C-A

38245227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158061732-C-G

38245407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158061821-G-A

38245540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158061928-A-G

38245596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158061982-C-G

38245607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158061994-G-A

38245778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158062168-T-C

38245778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158062168-T-G

http://identifiers.org/hco/20/GRCh38#38245832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158062222-C-A

38245832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158062222-C-T

38245896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158062285-T-C

38245922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 158062311-G-T

38245932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158062321-G-A

38245998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158062387-C-T

38246118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158062507-T-A

38246118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158062507-T-C

38246139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158062528-G-T

38246142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158062531-G-A

38246175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158062564-A-G

38246210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158062615-G-A

38246210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158062615-G-T

http://identifiers.org/hco/20/GRCh38#38246232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158062637-C-A

38246232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158062637-C-T

38246241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158062645-T-C

38247164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158062882-G-A

38247305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158062953-C-T

38247384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158063022-T-C

38247464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158063111-T-C

38249439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158063333-G-A

38249491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158063384-G-C

38249514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158063399-T-G

38249552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158063434-C-T

38249562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158063438-C-T

38249563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158063439-G-A

38249593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158063471-A-G

38249605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158063483-C-G

38249645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158063524-G-A

http://identifiers.org/hco/20/GRCh38#38249803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158063664-A-C

38252490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158064351-C-T

38252519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158064383-C-G

38252738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158064576-C-T

38252859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158064690-A-G

38253115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 158064929-G-C

38253567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158065521-C-T

38253612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158065558-C-T

38255281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158067180-A-G

38255505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158067354-C-T

38255864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158067695-A-G

38255929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158067756-C-G

38256190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158067978-C-T

38256931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158068320-C-T

38257093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158068459-G-C

38258903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158069513-T-C

38259101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158069699-A-T

38259257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158069868-G-C

38259333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158069935-C-T

38259348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158069947-T-C

38259496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158070019-T-C

38260056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158070482-T-A

38260056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158070482-T-C

38260081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158070517-G-A

38260081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158070517-G-T

38260111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158070561-T-C

38260179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158070656-C-T

http://identifiers.org/hco/20/GRCh38#38260364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158070836-C-A

38260381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158070853-T-A

38260381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158070853-T-C

38260532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158071014-C-G

38260586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158071054-C-T

38260613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158071079-A-G

38260621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158071087-G-A

38260621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158071087-G-T

http://identifiers.org/hco/20/GRCh38#38260625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158071091-A-C

38260625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158071091-A-G

http://identifiers.org/hco/20/GRCh38#38260628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158071094-C-A

38260628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158071094-C-G

38260628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158071094-C-T

http://identifiers.org/hco/20/GRCh38#38260629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158071095-C-A

38260639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158071105-G-A

38260639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158071105-G-C

38260639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158071105-G-T

38260715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158071167-G-A

38260715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158071167-G-C

38260715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158071167-G-T

http://identifiers.org/hco/20/GRCh38#38260772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158071213-C-A

38260772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158071213-C-G

38260772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158071213-C-T