http://identifiers.org/hco/7/GRCh38#138594429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37961293-C-A

138594429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 37961293-C-T

http://identifiers.org/hco/7/GRCh38#138594516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37961368-C-A

138594516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 37961368-C-T

138594517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 37961369-A-G

138594626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37961463-A-G

138595368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37961963-G-A

138595403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37961996-A-G

http://identifiers.org/hco/7/GRCh38#138595450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37962013-C-A

138595483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37962053-G-A

138595525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37962100-C-G

138595530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37962105-T-A

138595722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37962296-A-T

138596424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37963440-G-A

138596424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37963440-G-T

138596468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37963484-G-A

138596540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37963556-A-G

138596557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37963573-T-A

138596557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37963573-T-C

138596627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37963642-A-G

http://identifiers.org/hco/7/GRCh38#138596796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37963785-C-A

http://identifiers.org/hco/7/GRCh38#138596846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37963835-C-A

138596846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37963835-C-G

138596869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37963844-G-T

138596948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37963919-A-G

138596975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37963946-G-T

138597006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37963976-A-G

138599445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37965914-G-A

138599599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37966078-A-G

138615097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37984708-T-C

138615105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37984716-C-G

138615105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37984716-C-T

138615109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37984720-G-A

138615176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37984798-G-A

138616394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37985412-T-C

138616534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37985530-C-G

138616587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37985607-C-T

138616616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37985634-A-G

138617320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37985711-G-C

http://identifiers.org/hco/7/GRCh38#138618036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37986263-C-A

http://identifiers.org/hco/7/GRCh38#138618049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37986276-A-C

138618049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37986276-A-T

138620981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37988111-G-A

138620981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37988111-G-T

http://identifiers.org/hco/7/GRCh38#138621003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37988133-C-A

138621003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37988133-C-T

138621011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37988141-G-T

http://identifiers.org/hco/7/GRCh38#138621012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37988142-A-C

138621012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37988142-A-T

http://identifiers.org/hco/7/GRCh38#138621180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37988305-C-A

138621180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37988305-C-T

138621261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37988378-G-A

138625798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37989074-A-G

138625870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37989141-A-G

138625870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37989141-A-T

http://identifiers.org/hco/7/GRCh38#138625885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37989157-C-A

138625885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37989157-C-G

138625885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37989157-C-T

138625942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37989198-G-C

138626085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37989337-G-A

138626086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37989338-C-T

138626087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37989339-A-G

http://identifiers.org/hco/7/GRCh38#138626145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37989361-A-C

138626145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37989361-A-G

138626145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37989361-A-T

138627237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37991577-C-G

http://identifiers.org/hco/7/GRCh38#138627261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37991600-C-A

138627290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37991629-G-A

138627290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37991629-G-T

138627303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37991642-A-G

138627320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37991662-C-G

http://identifiers.org/hco/7/GRCh38#138627512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37991854-C-A

138627526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37991868-G-T

138627543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37991885-G-A

138627543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37991885-G-C

138627543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37991885-G-T

http://identifiers.org/hco/7/GRCh38#138627598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37991919-C-A

138627598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37991919-C-T

138627632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37991956-C-T

http://identifiers.org/hco/7/GRCh38#138628029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37993834-A-C

http://identifiers.org/hco/7/GRCh38#138628060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37993865-C-A

138628060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37993865-C-T

138628068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37993873-G-A

138628068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37993873-G-T

138628069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37993874-T-A

138628213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37994010-C-T

http://identifiers.org/hco/7/GRCh38#138628258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37994055-A-C

138628273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 37994070-A-G

138628380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994183-A-G

138628394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994197-A-G

138628394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994197-A-T

138628404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994204-C-T

138628406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994206-G-C

138628406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994206-G-T

http://identifiers.org/hco/7/GRCh38#138628407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37994207-A-C

138628407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994207-A-G

http://identifiers.org/hco/7/GRCh38#138628489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37994295-C-A

138628489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994295-C-T

http://identifiers.org/hco/7/GRCh38#138628491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37994297-C-A

138628491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994297-C-G

138628502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994308-A-G

http://identifiers.org/hco/7/GRCh38#138628511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37994315-A-C

138628514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994318-G-A

138628514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994318-G-T

138628515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994319-T-C

138628534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994334-A-T

138628666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994465-T-C

138628819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994838-T-A

138628886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994905-C-T

138628895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37994916-G-A

138629161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37995224-G-A

138629334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37995316-G-A

138629438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37995356-G-T

138629707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37995587-G-A

138629707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37995587-G-C

138629728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37995601-G-A

138629728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37995601-G-T

138629729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37995602-G-C

138629977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37995854-A-G

http://identifiers.org/hco/7/GRCh38#138630154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37996722-C-A

http://identifiers.org/hco/7/GRCh38#138630155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37996723-A-C

138630229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37996790-G-T

138630230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37996791-G-A

138630230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37996791-G-T

http://identifiers.org/hco/7/GRCh38#138630231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37996792-C-A

138630231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37996792-C-T

138641335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37998078-T-A

138641335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37998078-T-C

138644579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37998368-A-T

http://identifiers.org/hco/7/GRCh38#138644600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37998395-C-A

138644600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37998395-C-T

http://identifiers.org/hco/7/GRCh38#138644640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37998435-C-A

138644640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37998435-C-T

http://identifiers.org/hco/7/GRCh38#138644648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#37998443-C-A

138644759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 37998526-G-T

138644780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37998547-C-T

138644801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37998568-A-G

138644819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 37998586-A-G

138644909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37998665-T-C

138644980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37998732-T-A

138644980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37998732-T-C

138648949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37999870-G-T

138648993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37999913-G-A

138648993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 37999913-G-T

138649033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 37999950-G-C

138649152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38000069-G-A

138649152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38000069-G-C

138649152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38000069-G-T

138650221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38001249-G-A

138650354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38001390-G-A

138650354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38001390-G-C

138650374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38001409-T-C

http://identifiers.org/hco/7/GRCh38#138650464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38001500-C-A

138650464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38001500-C-T

138650831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38003305-G-T

138651130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38003597-G-A

http://identifiers.org/hco/7/GRCh38#138651209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38003676-C-A

http://identifiers.org/hco/7/GRCh38#138651345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38003758-A-C

138651345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38003758-A-G

138656606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38004042-T-C

http://identifiers.org/hco/7/GRCh38#138656609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38004045-A-C

138656609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38004045-A-G

http://identifiers.org/hco/7/GRCh38#138657772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38004901-C-A

138657810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38004938-A-G

http://identifiers.org/hco/7/GRCh38#138659869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38006531-C-A

138659869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 38006531-C-G

138659869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 38006531-C-T

138660021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38006684-T-C

http://identifiers.org/hco/7/GRCh38#138660281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38006871-C-A

http://identifiers.org/hco/7/GRCh38#138660285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38006875-C-A

138660301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38006891-T-C

138660332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38006922-A-T

138662972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38007858-G-T

http://identifiers.org/hco/7/GRCh38#138662997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38007884-A-C

138663083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 38007963-G-T

http://identifiers.org/hco/7/GRCh38#138663197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38008098-C-A

http://identifiers.org/hco/7/GRCh38#138663205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38008106-C-A

138663205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38008106-C-G

138663205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38008106-C-T

138663374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38008259-G-A

138663374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38008259-G-C

138663374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38008259-G-T

138663404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38008298-G-A

138663404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38008298-G-T

138663418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38008312-C-G

138663503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38008389-T-C

138663527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38008412-C-T

138671896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38013527-T-C

138671896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38013527-T-G

138671899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38013530-G-A

138671899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38013530-G-T

138671918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38013549-G-A

138671918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38013549-G-C

138671918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38013549-G-T

138671954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38013582-G-T

http://identifiers.org/hco/7/GRCh38#138671978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38013605-C-A

138671988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38013615-T-C

138672031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 38013660-T-A

http://identifiers.org/hco/7/GRCh38#138672135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38013766-C-A

138672135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38013766-C-T

http://identifiers.org/hco/7/GRCh38#138672163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38013792-A-C

138672194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38013815-T-C

138673125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38016868-T-A

138673125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38016868-T-C

138673158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38016904-G-A

http://identifiers.org/hco/7/GRCh38#138676832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38017852-C-A

138678557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38018130-C-G

138678557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38018130-C-T

138678566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38018139-G-A

138678566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38018139-G-T

http://identifiers.org/hco/7/GRCh38#138678668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38018179-C-A

138678668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38018179-C-T

138678829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38018288-C-T

http://identifiers.org/hco/7/GRCh38#138679144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38018643-C-A

138679144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38018643-C-T

http://identifiers.org/hco/7/GRCh38#138679159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38018658-C-A

138679159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38018658-C-T

138679625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38019111-C-T

138686930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38020927-T-C

138686930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38020927-T-G

138686937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38020934-T-C

138686976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38020977-A-G

138700831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38023164-A-G

138700956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38023299-G-T

138701090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38023775-C-T

138701144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38023827-A-G

138701144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: intron variant
orthologous variants: 38023827-A-T

138701184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5 prime UTR variant
orthologous variants: 38023857-A-G

138701226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27034
most severe consequence: 5 prime UTR variant
orthologous variants: 38023906-C-T