10679278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3 prime UTR variant
orthologous variants: 31274439-G-A

http://identifiers.org/hco/5/GRCh38#10679474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31274285-C-A

10679570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3 prime UTR variant
orthologous variants: 31274239-C-T

10679632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3 prime UTR variant
orthologous variants: 31274166-G-A

http://identifiers.org/hco/5/GRCh38#10679643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31274155-C-A

10679666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3 prime UTR variant
orthologous variants: 31274133-C-G

10679787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3 prime UTR variant
orthologous variants: 31274069-G-A

10679787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3 prime UTR variant
orthologous variants: 31274069-G-T

10679794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3 prime UTR variant
orthologous variants: 31274062-A-G

http://identifiers.org/hco/5/GRCh38#10679802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31274054-A-C

10679834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3 prime UTR variant
orthologous variants: 31274021-C-G

10679866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3 prime UTR variant
orthologous variants: 31273989-G-A

10679918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3 prime UTR variant
orthologous variants: 31273929-T-C

10679971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3 prime UTR variant
orthologous variants: 31273878-C-T

10679979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3 prime UTR variant
orthologous variants: 31273871-C-T

10680724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 31273802-T-G

10680793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 31273753-G-C

10680799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3_prime_UTR_variant, stop_gained
orthologous variants: 31273747-G-A

10680799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 31273747-G-T

http://identifiers.org/hco/5/GRCh38#10680831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31273714-C-A

10680842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 31273703-A-T

10680850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 31273695-T-A

10680858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 31273687-G-A

10680858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 31273687-G-C

10680885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 31273659-G-A

10680904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 31273640-A-G

10680927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 31273621-C-G

10680986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 31273557-G-A

10680986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 31273557-G-T

10681150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31273360-G-A

10681150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31273360-G-T

http://identifiers.org/hco/5/GRCh38#10681181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31273329-C-A

10681181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31273329-C-T

10682593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31273286-C-T

10682611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31273269-G-A

10682614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31273268-A-T

10682617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31273265-C-T

10682658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31273230-T-C

10682929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272966-G-A

http://identifiers.org/hco/5/GRCh38#10682955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31272936-C-A

10682955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272936-C-T

http://identifiers.org/hco/5/GRCh38#10682991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31272900-C-A

10683000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272888-G-T

10683495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31272623-G-A

10683514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31272604-C-T

10683530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 31272574-C-T

10683645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272462-T-C

10683645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272462-T-G

10683682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272432-A-G

10683689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272425-G-A

10683689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272425-G-T

http://identifiers.org/hco/5/GRCh38#10683699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31272414-C-A

http://identifiers.org/hco/5/GRCh38#10683700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31272413-C-A

10683700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272413-C-T

10683726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272388-C-T

10683811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272297-G-A

10683811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272297-G-C

10683814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272294-T-C

10685375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31270575-C-T

10685397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31270553-A-G

10685589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31270377-G-A

10685634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31270338-A-G

10685706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31270275-G-A

10685789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31270200-G-T

10685923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31270077-C-G

10685923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31270077-C-T

10685925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31270075-G-A

10685929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31270071-C-T

10689782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31268425-C-T

10690343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31267943-G-A

10691410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31267661-C-T

10691463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31267607-C-T

10691543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31267555-C-T

10691548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31267550-A-G

10691609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31267489-A-T

http://identifiers.org/hco/5/GRCh38#10691828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31267299-C-A

10691828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31267299-C-T

10694954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31265467-G-T

10695129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31265292-C-T

10695152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31265269-A-G

10695185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31265237-C-T

10695255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31265175-G-A

10696851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31263382-T-C

10696875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31263358-G-A

10696875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31263358-G-C

10696883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31263350-A-G

http://identifiers.org/hco/5/GRCh38#10696933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31263311-C-A

10696933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31263311-C-T

10697047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31263216-T-A

10697106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31263189-C-T

10697391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31262951-T-C

10697604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31262746-G-A

10697644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31262704-G-C

10697783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31262597-A-G

10697990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31262451-C-T

10698091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31262340-C-T

10698257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31262192-G-A

10698269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31262180-T-C

10698311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31262136-A-T

10698353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31262094-T-G

10698384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31262071-G-A

10698464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31261999-A-G

10699277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31261789-C-T

10699278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31261788-T-G

http://identifiers.org/hco/5/GRCh38#10699375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31261730-C-A

10699480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31261623-C-T

10699506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31261597-T-C

10699847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31261214-C-T

10700024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31260856-T-A

10700072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31260729-G-A

10700230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31260585-C-G

10700261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31260570-G-T

10700455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31260419-A-G

10700586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31260297-G-A

10700586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31260297-G-C

10700612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31260271-C-T

10700732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31260171-G-T

10700779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31260131-C-G

10700838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31260012-C-T

10700960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31259880-G-C

10700983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31259855-G-A

10701370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31259270-G-C

10701703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31258991-C-G

10702062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31258642-G-A

10702105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31258613-G-A

http://identifiers.org/hco/5/GRCh38#10702143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31258576-C-A

10703070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31257665-T-G

http://identifiers.org/hco/5/GRCh38#10703202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31257534-A-C

10703274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31257470-G-A

10703274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31257470-G-T

10703471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31257280-G-C

10703775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31257001-G-A

10703775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31257001-G-T

10703777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31256999-G-A

10708743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31255346-G-A

10708842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31255252-C-G

10708863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31255232-T-G

10708941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31255162-T-C

10709152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31254955-G-A

10709168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31254935-C-T

10709191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31254916-T-A

10709191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31254916-T-C

10709211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31254896-T-C

10709331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31254782-T-C

10709632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31254495-T-C

10713489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31254082-G-A

10713678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31253908-C-T

10713832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31253762-G-A

10713877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31253714-C-G

http://identifiers.org/hco/5/GRCh38#10715610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31253175-A-C

http://identifiers.org/hco/5/GRCh38#10715995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31252821-A-C

10716238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31252603-G-C

10716247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31252594-C-T

10722680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31252415-T-C

10722877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31252277-C-G

10722972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31252187-C-T

10723012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31252150-C-G

10723024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31252138-C-T

10723206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31251814-A-G

10723316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31251697-T-C

10723501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31251552-T-C

10723525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31251528-A-T

10723546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31251507-G-C

http://identifiers.org/hco/5/GRCh38#10723661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31251112-C-A

10723757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31251040-T-G

10723958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31250856-T-C

10725021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31249372-C-T

10725099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31249292-T-C

10725281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31249123-G-C

10725589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31248863-C-T

10725604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31248848-T-C

10725630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31248821-T-C

http://identifiers.org/hco/5/GRCh38#10725640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31248811-C-A

10725640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31248811-C-T

10726201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31248288-C-G

10726211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31248278-T-A

http://identifiers.org/hco/5/GRCh38#10726240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31248249-C-A

10726240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31248249-C-T

10726349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31248216-G-T

10726737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31248024-C-T

10726818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31247950-G-C

10726873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31247822-A-G

10727144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31247518-C-T

10727274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31247405-G-A

10727523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31247173-A-T

10727542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31247159-G-A

10727542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31247159-G-C

10731624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31244522-T-G

10731627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31244519-G-A

10731814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31244351-C-T

http://identifiers.org/hco/5/GRCh38#10732318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31243930-A-C

10732505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31243769-A-G

10732548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31243702-T-C

10732631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31243626-T-C

10732724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31243537-A-G

10732800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31243467-T-C

10732888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31243388-A-G

http://identifiers.org/hco/5/GRCh38#10733079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31243209-C-A

10733079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31243209-C-T

10733099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31243190-C-T

10733103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31243186-T-C

10733128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31243158-C-G

10733206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31243120-G-A

http://identifiers.org/hco/5/GRCh38#10733627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31242914-C-A

10733627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31242914-C-G

10733801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31242815-T-C

10733805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31242811-G-T

10733844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31242798-G-A

10733844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31242798-G-T

10733845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31242797-T-C

10733973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31242685-T-G

10734122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31242552-A-G

10734177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31242520-A-G

10734194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31242506-T-C

10734198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31242502-T-A

10734198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31242502-T-C

10734208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31242492-A-G

10734263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31242456-T-C

10734312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31242428-T-C

10734353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31242386-T-C

10734355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31242384-T-C

http://identifiers.org/hco/5/GRCh38#10734382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#31242354-C-A

10734393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31242345-G-A

10734393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31242345-G-T

http://identifiers.org/hco/5/GRCh38#10734418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#31242321-C-A

10734418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31242321-C-T

10734488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31242251-T-G

10734626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31242111-G-A

10734644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31242093-T-C

10734691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31242061-T-A

10734907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31241848-T-A

10734907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31241848-T-C

10734973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31241787-G-A

10734978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31241782-C-T

10735101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31241676-G-A

10735102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31241675-C-T

http://identifiers.org/hco/5/GRCh38#10735165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31241608-A-C

10735257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31241548-T-A

10735257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31241548-T-C

http://identifiers.org/hco/5/GRCh38#10735258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31241547-C-A

10735258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31241547-C-T

10735281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31241524-A-G

10735293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31241512-C-G

10735396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31241413-G-A

10735869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31240996-G-A

10735978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31240893-A-G

10736010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31240864-T-C

10736079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31240804-T-C

http://identifiers.org/hco/5/GRCh38#10736163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#31240721-C-A

10736163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31240721-C-T

10736264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31240631-T-C

10736326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31240587-A-T

10736332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31240581-C-T

10736488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31240472-G-A

10743945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31238431-T-C

10744001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31238376-A-G

http://identifiers.org/hco/5/GRCh38#10744853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31237681-C-A

10744888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31237658-G-A

10744947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31237604-G-T

10745035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31237537-A-T

10745068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31237504-G-A

10745239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31237333-A-G

10745240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31237332-T-C

http://identifiers.org/hco/5/GRCh38#10745303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31237255-C-A

10745464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31237122-G-C

http://identifiers.org/hco/5/GRCh38#10745489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31237095-C-A

10745521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31237063-C-T

10747600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31236470-G-A

http://identifiers.org/hco/5/GRCh38#10747630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31236442-A-C

10747704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31236371-G-A

10747805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31236270-G-T

http://identifiers.org/hco/5/GRCh38#10747815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31236258-C-A

10747972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31236194-G-T

10748001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31236165-T-C

10748002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31236164-C-G

http://identifiers.org/hco/5/GRCh38#10748022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31236150-C-A

10748022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31236150-C-T

10748026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31236146-T-C

10748122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31236061-A-T

10748131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31236052-G-C

10748131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31236052-G-T

10748141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31236044-A-G

10748149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31236036-C-T

10748152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31236035-A-G

10748156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31236031-G-A

10748156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31236031-G-T

10748229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31235959-G-A

10748288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31235900-G-C

10748302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31235886-T-C

10748304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31235884-T-A

10748304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31235884-T-C

http://identifiers.org/hco/5/GRCh38#10748360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31235838-A-C

10748360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31235838-A-T

10748361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31235837-G-T

10748400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31235813-G-A

10748407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31235806-T-C

10748427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31235786-G-A

http://identifiers.org/hco/5/GRCh38#10748810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31235255-A-C

10748810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31235255-A-G

http://identifiers.org/hco/5/GRCh38#10748952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31235153-A-C

10748952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31235153-A-G

10749135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31234977-G-A

10749223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31234900-C-T

http://identifiers.org/hco/5/GRCh38#10749367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31234763-C-A

10751141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31232101-G-T

10751160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31232078-T-C

10751287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31231948-A-G

10751603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31231724-T-C

10751661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31231675-T-C

10751856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31231500-T-C

10751995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31231416-C-T

10752116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31231293-G-A

10752151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31231255-C-T

10752152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31231254-C-T

10752159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31231252-G-C

http://identifiers.org/hco/5/GRCh38#10752488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31230950-C-A

10752655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31230798-T-C

10752736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31230781-G-A

10752831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31230700-C-T

10753251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31229879-G-C

http://identifiers.org/hco/5/GRCh38#10753474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31229682-A-C

10753640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31229514-G-C

10753718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31229429-A-G

10753780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31229365-G-A

10753795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31229350-T-C

10755777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31228872-C-T

10756265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31228708-G-A

10756346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31228620-T-A

10756388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31228563-A-G

10756493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31228462-T-C

http://identifiers.org/hco/5/GRCh38#10756546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31228411-C-A

10756546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31228411-C-T

10756770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31228180-G-C

10756832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31228139-T-C

10757581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31227766-A-T

10757719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31227630-G-A

10757763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31227602-G-A

10757763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31227602-G-C

10757790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31227584-T-C

10757827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31227569-G-C

10757885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31227484-T-C

http://identifiers.org/hco/5/GRCh38#10757914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31227462-A-C

10758204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31227191-G-A

10758204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31227191-G-T

10759254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31226316-T-C

10759271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31226300-C-G

10759271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31226300-C-T

10760225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31225373-G-A

http://identifiers.org/hco/5/GRCh38#10760454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31225149-C-A

10760497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31225107-T-C

10760778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31224864-G-A

10760778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31224864-G-C

10760779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31224863-T-C

10760779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31224863-T-G

10760817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31224844-G-A

http://identifiers.org/hco/5/GRCh38#10760872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31224815-C-A

10760872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31224815-C-G

10760872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31224815-C-T

10760886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31224797-G-A

10760886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31224797-G-C

10760886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31224797-G-T

10760887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31224796-G-A

10760887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31224796-G-C

10760887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31224796-G-T

http://identifiers.org/hco/5/GRCh38#10760909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31224774-C-A

10760938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31224772-A-G

10760938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31224772-A-T

http://identifiers.org/hco/5/GRCh38#10760943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31224767-C-A

10760943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31224767-C-T

10761023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31224718-G-A

10761023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31224718-G-T

10761074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31224667-G-A

10761074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31224667-G-T

http://identifiers.org/hco/5/GRCh38#10761122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31224628-C-A

10761122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31224628-C-G

10761122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31224628-C-T

10761156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31224604-G-A

10761156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31224604-G-C

10761156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31224604-G-T

10761157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31224603-G-A

10761157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31224603-G-T

10761174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31224592-A-G

10761188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31224584-G-A

10761188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31224584-G-T

http://identifiers.org/hco/5/GRCh38#10761231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31224556-C-A

10761231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31224556-C-G

10761231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31224556-C-T